A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism

Decreased Spontaneous Attention to Social Scenes in 6-Month-Old Infants Later Diagnosed with Autism Spectrum Disorders

(2013) Katarzyna Chawarska et al.   BIOLOGICAL PSYCHIATRY

Speech Disturbs Face Scanning in 6-Month-Old Infants Who Develop Autism Spectrum Disorder

(2013) Frederick Shic et al.   BIOLOGICAL PSYCHIATRY

Genetic causes of developmental disorders

(2013) Jacob A.S. Vorstman et al.   CURRENT OPINION IN NEUROLOGY

Family-based association tests for sequence data, and comparisons with population-based association tests

(2013) Iuliana Ionita-Laza et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Roles of Rho GTPases in Intracellular Transport and Cellular Transformation

(2013) Xiaojuan Chi et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Comparison of Bumetanide- and Metolazone-Based Diuretic Regimens to Furosemide in Acute Heart Failure

(2013) Tien M. H. Ng et al.   JOURNAL OF CARDIOVASCULAR PHARMACOLOGY AND THERAPEUTICS

Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency and/or congenital malformations

(2013) Caroline Schluth-Bolard et al.   JOURNAL OF MEDICAL GENETICS

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

(2013)   LANCET

Attention to eyes is present but in decline in 2–6-month-old infants later diagnosed with autism

(2013) Warren Jones et al.   NATURE

Autism-Associated Neuroligin-3 Mutations Commonly Disrupt Tonic Endocannabinoid Signaling

(2013) Csaba Földy et al.   NEURON

Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

(2013) Timothy W. Yu et al.   NEURON

From single-SNP to wide-locus: genome-wide association studies identifying functionally related genes and intragenic regions in small sample studies

(2013) Knut M Wittkowski et al.   PHARMACOGENOMICS

The Brain’s Response to the Human Voice Depends on the Incidence of Autistic Traits in the General Population

(2013) Yuko Yoshimura et al.   PLoS One

O-GlcNAc transferase (OGT) as a placental biomarker of maternal stress and reprogramming of CNS gene transcription in development

(2013) C. L. Howerton et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment

(2013) C. A. Rietveld et al.   SCIENCE

Mechanisms and effects of seizures in the immature brain

(2013) Romain Nardou et al.   Seminars in Fetal & Neonatal Medicine

Local Functional Overconnectivity in Posterior Brain Regions Is Associated with Symptom Severity in Autism Spectrum Disorders

(2013) Christopher Lee Keown et al.   Cell Reports

Brain Hyperconnectivity in Children with Autism and its Links to Social Deficits

(2013) Kaustubh Supekar et al.   Cell Reports

All SNPs Are Not Created Equal: Genome-Wide Association Studies Reveal a Consistent Pattern of Enrichment among Functionally Annotated SNPs

(2013) Andrew J. Schork et al.   PLoS Genetics

Autism-specific maternal autoantibodies recognize critical proteins in developing brain

(2013) D Braunschweig et al.   Translational Psychiatry

Scan-Statistic Approach Identifies Clusters of Rare Disease Variants in LRP2, a Gene Linked and Associated with Autism Spectrum Disorders, in Three Datasets

(2012) Iuliana Ionita-Laza et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Five Years of GWAS Discovery

(2012) Peter M. Visscher et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Moesin Is a Glioma Progression Marker That Induces Proliferation and Wnt/ -Catenin Pathway Activation via Interaction with CD44

(2012) X. Zhu et al.   CANCER RESEARCH

Infant Neural Sensitivity to Dynamic Eye Gaze Is Associated with Later Emerging Autism

(2012) Mayada Elsabbagh et al.   CURRENT BIOLOGY

Genetic architecture in autism spectrum disorder

(2012) Bernie Devlin et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Individual common variants exert weak effects on the risk for autism spectrum disorders

(2012) Richard Anney et al.   HUMAN MOLECULAR GENETICS

Mutations inSYNGAP1Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency

(2012) Martin H. Berryer et al.   HUMAN MUTATION

Microtubule stability, Golgi organization, and transport flux require dystonin-a2–MAP1B interaction

(2012) Scott D. Ryan et al.   JOURNAL OF CELL BIOLOGY

Ca2+-activated Cl- channels at a glance

(2012) J. Berg et al.   JOURNAL OF CELL SCIENCE

Vps10 Family Proteins and the Retromer Complex in Aging-Related Neurodegeneration and Diabetes

(2012) R. F. Lane et al.   JOURNAL OF NEUROSCIENCE

FMRP targets distinct mRNA sequence elements to regulate protein expression

(2012) Manuel Ascano et al.   NATURE

Membrane Progesterone Receptors: Evidence for Neuroprotective, Neurosteroid Signaling and Neuroendocrine Functions in Neuronal Cells

(2012) Peter Thomas et al.   NEUROENDOCRINOLOGY

Mitochondrial Dysfunction in Pten Haplo-Insufficient Mice with Social Deficits and Repetitive Behavior: Interplay between Pten and p53

(2012) Eleonora Napoli et al.   PLoS One

Paternal Age and Risk of Autism in an Ethnically Diverse, Non-Industrialized Setting: Aruba

(2012) Ingrid D. C. van Balkom et al.   PLoS One

CNTNAP2 is significantly associated with schizophrenia and major depression in the Han Chinese population

(2012) Weidong Ji et al.   PSYCHIATRY RESEARCH

A Noncoding RNA Antisense to Moesin at 5p14.1 in Autism

(2012) T. Kerin et al.   Science Translational Medicine

What does CNTNAP2 reveal about autism spectrum disorder?

(2012) Olga Peñagarikano et al.   TRENDS IN MOLECULAR MEDICINE

An Autism-Associated Variant of Epac2 Reveals a Role for Ras/Epac2 Signaling in Controlling Basal Dendrite Maintenance in Mice

(2012) Deepak P. Srivastava et al.   PLOS BIOLOGY

Autism genetics: searching for specificity and convergence

(2012) Jamee M Berg et al.   GENOME BIOLOGY

Common genetic variants, acting additively, are a major source of risk for autism

(2012) Lambertus Klei et al.   Molecular Autism

Matrix Metalloproteinases and Minocycline: Therapeutic Avenues for Fragile X Syndrome

(2012) Saul S. Siller et al.   NEURAL PLASTICITY

A randomised controlled trial of bumetanide in the treatment of autism in children

(2012) E Lemonnier et al.   Translational Psychiatry

Calcium-activated chloride current expression in axotomized sensory neurons: what for?

(2012) Mathieu Boudes et al.   Frontiers in Molecular Neuroscience

Genetic and Epigenetic Networks in Intellectual Disabilities

(2011) Hans van Bokhoven   Annual Review of Genetics

Early Brain Overgrowth in Autism Associated With an Increase in Cortical Surface Area Before Age 2 Years

(2011) Heather Cody Hazlett et al.   ARCHIVES OF GENERAL PSYCHIATRY

Early Generalized Overgrowth in Boys With Autism

(2011) Katarzyna Chawarska   ARCHIVES OF GENERAL PSYCHIATRY

Male predominance in autism: neuroendocrine influences on arousal and social anxiety

(2011) Donald W. Pfaff et al.   Autism Research

EEG complexity as a biomarker for autism spectrum disorder risk

(2011) William Bosl et al.   BMC Medicine

Neural Correlates of Familiar and Unfamiliar Face Processing in Infants at Risk for Autism Spectrum Disorders

(2011) Rhiannon J. Luyster et al.   BRAIN TOPOGRAPHY

MMP-9 induces CD44 cleavage and CD44 mediated cell migration in glioblastoma xenograft cells

(2011) Chandramu Chetty et al.   CELLULAR SIGNALLING

Retracted: Association of upregulated Ras/Raf/ERK1/2 signaling with autism

(2011) H. Zou et al.   GENES BRAIN AND BEHAVIOR

The X-linked intellectual disability protein IL1RAPL1 regulates excitatory synapse formation by binding PTPδ and RhoGAP2

(2011) Pamela Valnegri et al.   HUMAN MOLECULAR GENETICS

GRK5 promotes F-actin bundling and targets bundles to membrane structures to control neuronal morphogenesis

(2011) Yuejun Chen et al.   JOURNAL OF CELL BIOLOGY

Onset Patterns in Autism: Correspondence Between Home Video and Parent Report

(2011) Sally Ozonoff et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

Exome sequencing identifies GRIN2A as frequently mutated in melanoma

(2011) Xiaomu Wei et al.   NATURE GENETICS

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

(2011) Stephan J. Sanders et al.   NEURON

Media Use by Children Younger Than 2 Years

(2011)   PEDIATRICS

Anoctamins

(2011) Karl Kunzelmann et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

Phenotype Restricted Genome-Wide Association Study Using a Gene-Centric Approach Identifies Three Low-Risk Neuroblastoma Susceptibility Loci

(2011) Lễ B. Nguyễn et al.   PLoS Genetics

Medicinal Chemistry of Competitive Kainate Receptor Antagonists

(2010) Ann M. Larsen et al.   ACS Chemical Neuroscience

A Versatile Gene-Based Test for Genome-wide Association Studies

(2010) Jimmy Z. Liu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism

(2010) I Filges et al.   CLINICAL GENETICS

A genome-wide scan for common alleles affecting risk for autism

(2010) R. Anney et al.   HUMAN MOLECULAR GENETICS

Flufenamic acid decreases neuronal excitability through modulation of voltage-gated sodium channel gating

(2010) Hau-Jie Yau et al.   JOURNAL OF PHYSIOLOGY-LONDON

Functional impact of global rare copy number variation in autism spectrum disorders

(2010) Dalila Pinto et al.   NATURE

A coding-independent function of gene and pseudogene mRNAs regulates tumour biology

(2010) Laura Poliseno et al.   NATURE

The protein tyrosine phosphatases PTPRZ and PTPRG bind to distinct members of the contactin family of neural recognition molecules

(2010) S. Bouyain et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Rapamycin for treating Tuberous sclerosis and Autism spectrum disorders

(2010) Dan Ehninger et al.   TRENDS IN MOLECULAR MEDICINE

Contactins

(2010) Yasushi Shimoda et al.   Cell Adhesion & Migration

A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1

(2009) Deqiong Ma et al.   ANNALS OF HUMAN GENETICS

Flufenamic acid suppresses epileptiform activity in hippocampus by reducing excitatory synaptic transmission and neuronal excitability

(2009) Miriam Fernández et al.   EPILEPSIA

Comparisons of multi-marker association methods to detect association between a candidate region and disease

(2009) David H. Ballard et al.   GENETIC EPIDEMIOLOGY

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism

(2009) R. A. Kumar et al.   JOURNAL OF MEDICAL GENETICS

A genome-wide linkage and association scan reveals novel loci for autism

(2009) Lauren A. Weiss et al.   NATURE

Common genetic variants on 5p14.1 associate with autism spectrum disorders

(2009) Kai Wang et al.   NATURE

Chloride channels as drug targets

(2009) Alan S. Verkman et al.   NATURE REVIEWS DRUG DISCOVERY

Common Genetic Variation and Human Traits

(2009) David B. Goldstein   NEW ENGLAND JOURNAL OF MEDICINE

Involvement of Members of the Cadherin Superfamily in Cancer

(2009) G. Berx et al.   Cold Spring Harbor Perspectives in Biology

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

(2008) Dan E. Arking et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic Calcium Signaling Abnormalities in the Central Nervous System: Seizures, Migraine, and Autism

(2008) J. Jay Gargus   Annals of the New York Academy of Sciences

Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder

(2008) Susan L. Christian et al.   BIOLOGICAL PSYCHIATRY

Progesterone receptors: Form and function in brain

(2008) Roberta Diaz Brinton et al.   FRONTIERS IN NEUROENDOCRINOLOGY

How to Interpret a Genome-wide Association Study

(2008) Thomas A. Pearson   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Ras Signaling Mechanisms Underlying Impaired GluR1-Dependent Plasticity Associated with Fragile X Syndrome

(2008) H. Hu et al.   JOURNAL OF NEUROSCIENCE

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

(2008) Mark I. McCarthy et al.   NATURE REVIEWS GENETICS

GABAA receptor trafficking and its role in the dynamic modulation of neuronal inhibition

(2008) Tija C. Jacob et al.   NATURE REVIEWS NEUROSCIENCE

Acute treatment and prevention of menstrually related migraine headache: Evidence-based review

(2008) T. Pringsheim et al.   NEUROLOGY

A Functional Genetic Link between Distinct Developmental Language Disorders

(2008) Sonja C. Vernes et al.   NEW ENGLAND JOURNAL OF MEDICINE

Bumetanide enhances phenobarbital efficacy in a neonatal seizure model

(2007) Volodymyr I. Dzhala et al.   ANNALS OF NEUROLOGY

Prioritized Subset Analysis: Improving Power in Genome-wide Association Studies

(2007) Chun Li et al.   HUMAN HEREDITY